100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
GCO570 - Midterm Questions and answers CA$16.55   Add to cart

Exam (elaborations)

GCO570 - Midterm Questions and answers

 0 view  0 purchase

GCO570 - Midterm Questions and answers

Preview 3 out of 25  pages

  • July 5, 2024
  • 25
  • 2023/2024
  • Exam (elaborations)
  • Questions & answers
All documents for this subject (166)
avatar-seller
stephanvdb04
GCO570 - Midterm
15y/o referred to genetics for hypermobility. Previously diagnosed with

✅✅
Autism. Noted to have macrocephaly, penile freckling, and hypermobile
joints - -PTEN Hamartoma Syndrome

GT: Sequencing PTEN gene

Referral: Oncology

Management:
- At 15 = ultrasound of thyroid
- Future = colon, kidney, and breast screening

27y/o male recently presented with unsteady gait, bradykinesia,
unresponsiveness, and decreased facial expression. Mild atrophy of the

✅✅
cerebrum and cerebellum was detected on brain MRI. -
-Early-Onset Parksinson's Disease; AD/AR (dependant on
age-onset)

GT: multi-gene panel

Referrals: Psychiatics

32-week premature delivery due to placental abruption with crash
C-section. Born to 33 y/o G1 P0 mother, who had history of gradual
onset of muscle weakness during the pregnancy. She had
polyhydramnios on ultrasound, but no other abnormal labs.

Male delivered due to no heart sounds or respirations. Apgars of 1.0.2.4
Hypotonic with no responsiveness to stimulation. Ultimately resuscitated,

✅✅
placed on respiratory support. Required G tube for feeding support and
eventually was able to go home on oxygen. - -Myotonic Dystrophy;
"floppy baby"; CTG repeats in DMPK gene; AD

More likely to expand from mom

GT: Repeat analysis

,Referrals: PT

3y/o female patient. Since birth she has been hypotonic and was behind
in her motor and speech milestones. During the appointment, you notice
the patient is having random eye movements and repeatedly thrusts her
head forward.

✅✅
You see that she has already been to Neurology and had an MRI which
showed a "molar tooth sign". - -Jourbert Syndrome; AR(30)/XL(1)

GT: Panel testing

4y/o patent recently referred for genetics evaluation due to the concern
for gross motor delay Patient had trouble learning to run. Parents have

✅✅
recently noticed he seems to tire more quickly than his peers and is
having trouble with stairs. - -Duchenne Muscular Dystrophy; DMD;
XL

GT: CMA/deldup analysis needed (majority)

Referral: CARDIO!

A 1.5 year old male presents to the hospital with a prolonged focal
seizure in the setting of a febrile illness. He had shaking of the left
hemibody lasting for 2 hours.

Family recently moved from out of state and had been given rescue
medications after he was diagnosed with "febrile seizures" at 7 months
of age. This is his 3rd hospitalization now for febrile status epilepticus.

Family reports prior work up including MRI and EEG in the past were
normal after his first seizure. No further work up has been pursued.

He's the product of a term pregnancy and delivery and was
developmentally normal until about 6 months when he started to fall
behind. He just started walking and has about 5 words.

, Recently family reports he will randomly jerk his whole body which is

✅✅
new over the past few months. This happens a few times per day. -
-Dravet Syndrome

GT: Panel

Referral: Neurology

Management: AAV Vector (1 time delivery) or ASO (anti-sense
oligonucleotide); no sodium blockers

A 2 year-old presents to the clinic with a known history of epilepsy for a
second opinion. She has multiple seizure types including initial onset of
convulsions at 5 months of age.

Currently her major seizure types include absence seizures (beginning
at age 1.5yo), myoclonic and atonic seizures. She has been on 5 anti-
seizure medications, but never obtained complete control.

She is the product of a term pregnancy and delivery however has had
global developmental delay and began walking at 20 months and still
has no words. There is concern for an underlying Autism Spectrum
Disorder, but she has not been formally diagnosed.


✅✅
Pediatrician has been concerned regarding a slowed head
circumference - -GLUT 1 Transported Deficiency; AD (most de
novo)

GT: normal blood glucose - low CSF glucose concentration + single
gene sequencing (SLC2A1)

Referral: Dietician

Management: Keto diet

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller stephanvdb04. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for CA$16.55. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

70055 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
CA$16.55
  • (0)
  Add to cart